Materiali e Metodi <ol><li> Ceppi di lievito <ul><li> Tutti i ceppi utilizzati in questo studio si basano sullo sfondo BY4742. Ceppo di controllo SILAC (Mat uno, his3, leu2, ura3, lys2 e Arg4:: G418) è stata fatta con l&#39;accoppiamento Arg4 ceppo cancellazione (Mat uno, his3, ura3, leu2 e Arg4:: G418) per BY4742 (Mat alfa, his3, leu2, ura3 e lys2), e la haploids meiotico sono stati ottenuti mediante dissezione tetrade. Pertanto, il ceppo di controllo è un auxotroph di lisina e arginina. Il ceppo esca è stata fatta da PCR-mediata ricombinazione omologa con il vettore pBS1479. Pertanto, il tag epitopo utilizzato in questo studio è la purificazione di affinità tandem (TAP) tag (3). </li></ul></li><li> SILAC: <ul><li> Il ceppo di controllo SILAC è stato coltivato in mezzi di abbandono minimale integrato con il 98% di L-lisina-4 ,4,5,5-D4 (0,03 g / L, Cambridge Isotope) e il 98% di L-arginina-13 C 6 (0,036 g / L, Cambridge Isotope). </li><li> Il ceppo è stato coltivato in esca regolarmente medio ricco di acidi normale isotopica aminoacidi. </li></ul></li><li> Prima tappa di purificazione TAP [Questo protocollo è stato adattato dal Cold Spring Harbor corso manuale di laboratorio (4)] ** La notte prima della purificazione, pre-chill mortaio e pestello in freezer -80 ° C. Inoltre, pre-chill un bicchiere a -20 ° C ** Rendono questi buffer a destra prima di utilizzare (per 1 L di cultura): <ul><li> 30 ml di buffer NP-40 con 25 microlitri PIC (1 / 2000), 50 ml di 1M DTT </li><li> 20 ml di NP-40 buffer con 1 / 200 PIC, 50 ml di 1M DTT </li><li> 10 ml di TEV-C buffer con 1 / 2000 PIC, 10 ml di 1 M DTT </li></ul></li></ol> SILAC e la preparazione <ol><li> Grow 1L ogni ceppo esca e il controllo ceppo separatamente per OD 600 = 1,0-1,3. </li><li> Versare la cultura in 500 ml provette Nalgene. Bilanciare il carico e le celle a pellet 2580X g. </li><li> Decantare i media e risospendere pellet con 50 ml di freddo dH 2 O durante il trasferimento alle cellule di provette da 50 ml. Pellet di cellule. ** È possibile congelare il pellet a -80 ° C ** </li><li> ** Importante ** corrispondere alla cultura ceppo di controllo alla cultura esca ceppo in 1:1 da peso a secco a pellet. </li><li> Risospendere ogni pellet di cellule in 10 ml di NP-40 buffer con Cocktail proteasi 1 / / 2000 Inhibitor (PIC). </li><li> Mescolare le due colture cellulari direttamente decantazione un tubo all&#39;altro. Macinazione </li><li> Versare il liquido N 2 nel pre-raffreddata malta e lasciarlo evaporare completamente. Aggiungere 2 ml di cellule al mortaio in movimento circolare. Versare qualche liquido N 2 per congelare le cellule. Macinare le cellule fino a quando le cellule diventano polvere fine. Ripetere il processo fino a quando tutte le cellule sono a terra. ** Non permettere alle cellule di disgelo. Aggiungi N 2 liquido quando necessario ** </li><li> Trasferire la polvere ad un bicchiere ghiacciato e scongelare a temperatura ambiente. Quando i bordi iniziano a sciogliersi, aggiungere 20 ml di NP-40 buffer con 1 / 200 PIC. </li><li> Trasferimento lisato greggio a 40 ml, tubi Nalgene. Girano a 39000 xgfor 30 min. </li><li> In attesa, prendere 300 ml di Sepharose perline 2B (GE). Lavare le perline in 300 ml di NP-40 tampone (1 / 2, 000 PIC) 3 volte. Risospendere le sfere in 300 microlitri di buffer in modo che siano in liquame 1:1. Pre-clearing lisato cellulare </li><li> Trasferire il surnatante in una nuova provetta e aggiungere le perline 2B Sepharose. Incubare su una piattaforma rotante in camera fredda per 30 minuti. </li><li> In attesa, prendere 300 ml di IgG Sepharose 6 perline (GE). Lavare le perline in 300 ml di NP-40 tampone (1 / 2, 000 PIC) 3 volte. Risospendere le sfere in 300 _l tampone in modo che siano in liquame 1:1. </li><li> Pellet le perline. Trasferire il surnatante in una nuova provetta. ** Salva un&#39;aliquota del lisato cellulare di Western Blotting in seguito ** Legame con IgG perline sefarosio </li><li> Rimuovere le perle 2B Sepharose da centrifuga. Aggiungere le perline IgG (precedentemente preparato in 1:1 liquami). Separare il contenuto in due tubi per il legame più efficiente. Incubare su una piattaforma rotante in camera fredda per 2 ore. </li><li> Spin giù le perline. ** Salva una aliquota della fazione non legato ** </li><li> Lavare le perline con 10 ml di NP-40 tampone (1 / 2, 000 PIC). </li><li> Lavare perline con 3 ml di buffer TEV-C (1 / 2, 000 PIC). ** Salva una aliquota delle perline. Questo riflette l&#39;efficienza della ** vincolante Eluizione di perle IgG per scissione della proteasi TEV </li><li> Aggiungere 5 ml di AcTEV a 1 ml di TEV-C buffer (con 1 / 2, 000 PIC). Dopo la miscelazione, separare il contenuto in due provette Eppendorf da 1,5 ml per più efficiente miscelazione. Incubare su una piattaforma rotante in camera fredda durante la notte. </li><li> Spin giù le perline e trasferire l&#39;eluato in una nuova 1,5 ml di tubo. Lavare le perline con l&#39;aggiunta di 0,5 ml di TEV-C tampone </li><li> Combinare i elaute in una provetta. Si dovrebbe avere 1,5 ml di eluato in totale.** Salva un&#39;aliquota del eluato TEV ** Acido tricloroacetico (TCA) precipatation (Per l&#39;analisi spettrometria di massa a base, si consiglia di utilizzare EtOH / precipitazione acetato) </li><li> Regolare aliquote al 25% TCA con il 100% TCA. Per fare questo, separato da 1,5 ml di eluato in 2 tubi da 750 microlitri ciascuno. Aggiungere 250 ml di 100% TCA al tubo. La vostra soluzione dovrebbe diventare lattiginoso. </li><li> Mettere in ghiaccio per 30 minuti con vortex periodica. </li><li> Girare alla massima velocità nel tavolo centrifuga in camera fredda per 30 minuti. </li><li> Lavare una volta con 500 ml di ghiacciata acetone contenente lo 0,05 N HCl e girare per 5 minuti alla massima velocità (camera fredda). </li><li> Lavare una volta con 500 ml di acetone ghiacciata e girare per 5 min a max (camera fredda). </li><li> Rimuovere con cautela acetone e asciugare pellet. </li><li> Per la colorazione argento, risospendere il pellet in 50 ml di tampone 1X campione SDS. EtOH precipatation / acetato </li><li> Aggiungere 20 mg di glicogeno </li><li> Diluire i campioni 5X con il 100% EtOH e regolare a 50 mm dopo le 3 COO con uno stock di 2,5 M, pH 5,0 </li><li> Stare la soluzione per 2 ore </li><li> Pellet precipitato proteina mediante centrifugazione per 10 min a 12.000 g X a temperatura ambiente. </li></ol> NP-40 Buffer (per 200 ml) <table border="0"><tbody><tr><td></td><td> Magazzino concentrazione </td><td> Aggiungere </td></tr><tr><td> 10 mM tampone fosfato di sodio (pH 7,2) </td><td> 0,1 M </td><td> 20 ml </td></tr><tr><td> 150 mM NaCl </td><td> 2 M </td><td> 15 ml </td></tr><tr><td> 1% NP-40 </td><td> 100% </td><td> 2 ml </td></tr><tr><td> 50 mM NaF </td><td> 1 M </td><td> 10 ml </td></tr><tr><td> 0.1 mM Na 3 VO 4 </td><td> 10 mM </td><td> 2 ml </td></tr><tr><td style="text-align:right;" colspan="3"> Volume a 200 ml </td></tr></tbody></table> ADD prima dell&#39;uso: <ol><li> 1 / 1, 000 di 1 M DTT </li><li> 1 / 2, 000 di PIC (Inibitori della proteasi Cocktail) </li></ol> TEV-Buffer C (per 50 ml) <table border="0"><tbody><tr><td></td><td> Magazzino concentrazione </td><td> Aggiungere </td></tr><tr><td> 25 mM Tris (pH 8,0) </td><td> 100 mM </td><td> 12,5 ml </td></tr><tr><td> 150 mM NaCl </td><td> 2 M </td><td> 3,75 ml </td></tr><tr><td> 0,1% NP-40 </td><td> 100% </td><td> 50 _l </td></tr><tr><td> 0.5 mM EDTA </td><td> 500 mM </td><td> 50 __l </td></tr><tr><td style="text-align:right;" colspan="3"> Volume di 50 ml </td></tr></tbody></table> ADD prima dell&#39;uso: <ol><li> 1 / 1, 000 di 1M DTT </li><li> 1 / 2, 000 del PIC </li></ol>

<ol>
	<li>Loewen, C. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Inheritance+of+cortical+ER+in+yeast+is+required+for+normal+septin+organization.">Inheritance of cortical ER in yeast is required for normal septin organization.</a> Jour. Cell Biol. 179, 467-483 .</li><li>Ong, S., Foster, L. J., Hoog, C. L., Mann, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mass+spectrometric-based+approaches+in+quantitative+proteomics.">Mass spectrometric-based approaches in quantitative proteomics.</a> Methods. 29, 124-130 .</li><li>Puig, O. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+Tandem+Affinity+Purification+(TAP)+method:+a+general+procedure+of+protein+complex+purification.">The Tandem Affinity Purification (TAP) method: a general procedure of protein complex purification.</a> Methods. 24, 218-229 .</li><li>Amberg, D. C., Burke, D. J., Strathern, J. N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Methods+in+Yeast+Genetics.">Methods in Yeast Genetics.</a> , 123-125 .</li></ol>

Le aliquote salvati durante la procedura di purificazione dovrebbe includere (1) pre-cancellati lisato cellulare, (2) frazione legata, (3) frazione libera, e (4) frazione eluita. Si consiglia di analizzare il contenuto proteico del aliquote sopra mediante Western blotting utilizzando anticorpi anti-TAP o colorazione argento per riflettere l&#39;efficienza di legame e eluizione di questo esperimento. Esempi di un gel colorato d&#39;argento e una macchia sono mostrati in figura 1. Dal SILAC ci...

identification of protein complexes with quantitative proteomics in s. cerevisiae

I lipidi sono i componenti delle membrane cellulari che funzionano come barriere e nella compartimentazione dei processi cellulari, e di recente, come importanti molecole di segnalazione intracellulare. Tuttavia, a differenza delle proteine, i lipidi sono piccole molecole idrofobiche che il traffico principalmente da poco descritto percorsi nonvesicular, che si ipotizza che si verifichino presso i siti di contatto a membrana (MCS). MCS sono regioni in cui il reticolo endoplasmatico (ER) rende il contatto fisico diretto con una partnership organello, ad esempio, membrana plasmatica (PM). La porzione di ER ER-PM MCS è arricchita in lipidi sintetizzare gli enzimi, il che suggerisce che la sintesi dei lipidi si rivolge a questi siti e implicando che MCS sono importanti per il traffico dei lipidi. Il lievito è un modello ideale per studiare ER-PM MCS a causa della loro abbondanza, con oltre 1000 contatti per cella, e la loro natura conservata in tutti gli eucarioti. Scoprire le proteine ​​che costituiscono MCS è fondamentale per capire come si realizza il traffico lipidi nelle cellule, e come si comportano come molecole di segnalazione. Abbiamo trovato che un pronto soccorso chiamato Scs2p localizzare a ER-PM MCS ed è importante per la loro formazione. Il nostro obiettivo è scoprire i partner molecolari di Scs2p. L&#39;identificazione di complessi proteici si basa tradizionalmente sulla prima risolvere campioni di proteine ​​purificate mediante elettroforesi su gel, seguita da in-gel digestione delle bande proteiche e analisi dei peptidi mediante spettrometria di massa. Questo limita spesso lo studio di un piccolo sottoinsieme di proteine. Inoltre, complessi proteici sono esposti a denaturazione o non le condizioni fisiologiche durante la procedura. Per aggirare questi problemi, abbiamo realizzato un grande tecnica proteomica quantitativa per estrarre i dati imparziale e quantificati. Noi usiamo l&#39;etichettatura degli isotopi stabili di aminoacidi nelle cellule in coltura (SILAC) per incorporare i nuclei di base di isotopi di proteine ​​in un ceppo di controllo senza tag. Volumi uguali di cultura tag e senza tag, la cultura SILAC marcati sono mescolati insieme e lisate dalla macinazione in azoto liquido. Abbiamo poi effettuare una procedura di purificazione di affinità di abbattere complessi proteici. Infine, precipitare il campione, che è pronto per l&#39;analisi ad alte prestazioni cromatografia liquida / spettrometria di massa tandem. Ma soprattutto, proteine ​​del ceppo di controllo sono etichettati dai isotopo pesante e produrranno una massa / carica spostamento che può essere quantificata contro le proteine ​​senza etichetta nel ceppo esca. Pertanto, contaminanti, o legame aspecifici possono essere facilmente eliminati. Utilizzando questo approccio, abbiamo individuato diverse nuove proteine ​​che localizzano a ER-PM MCS. Presentiamo qui una descrizione dettagliata del nostro approccio.

Watch this Scientific Journal Video about Identification of protein complexes with quantitative proteomics in S. cerevisiae at JoVE.com

Identification of protein complexes with quantitative proteomics in S. cerevisiae

Qui si descrive una nuova tecnica di proteomica quantitativa per identificare i complessi proteici in Saccharomyces cerevisiae. In questo studio, abbiamo utilizzato il metodo SILAC insieme purificazione di affinità seguita dalla spettrometria di massa tandem per identificare con elevata specificità dei partner legame di una proteina ER, Scs2p.

L&#39;identificazione di complessi proteici con la proteomica quantitativa in S. cerevisiae

Lipids are the building blocks of cellular membranes that function as barriers and in compartmentalization of cellular processes, and recently, as ...

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Biology

13.1K Views.  University of British Columbia - UBC. Qui si descrive una nuova tecnica di proteomica quantitativa per identificare i complessi proteici in Saccharomyces cerevisiae. In questo studio, abbiamo utilizzato il metodo SILAC insieme purificazione di affinità seguita dalla spettrometria di massa tandem per identificare con elevata specificità dei partner legame di una proteina ER, Scs2p.

Video: Identification of protein complexes with quantitative proteomics in S. cerevisiae

Assay for Adhesion and Agar Invasion in S. cerevisiae

Yeasts are found in natural biofilms, where many microorganisms colonize surfaces. In artificial environments, such as surfaces of man-made objects, biofilms can reduce industrial productivity, destroy structures, and threaten human life. 1-3 On the other hand, harnessing the power of biofilms can help clean the environment and generate sustainable energy. 4-8
The ability of S. cerevisiae to colonize surfaces and participate in complex biofilms was mostly ignored until the rediscovery of the differentiation programs triggered by various signaling pathways and environmental cues in this organism. 9, 10 The continuing interest in using S. cerevisiae as a model organism to understand the interaction and convergence of signaling pathways, such as the Ras-PKA, Kss1 MAPK, and Hog1 osmolarity pathways, quickly placed S. cerevisiae in the junction of biofilm biology and signal transduction research. 11-20 To this end, differentiation of yeast cells into long, adhesive, pseudohyphal filaments became a convenient readout for the activation of signal transduction pathways upon various environmental changes. However, filamentation is a complex collection of phenotypes, which makes assaying for it as if it were a simple phenotype misleading. In the past decade, several assays were successfully adopted from bacterial biofilm studies to yeast research, such as MAT formation assays to measure colony spread on soft agar and crystal violet staining to quantitatively measure cell-surface adherence. 12, 21 However, there has been some confusion in assays developed to qualitatively assess the adhesive and invasive phenotypes of yeast in agar.
Here, we present a simple and reliable method for assessing the adhesive and invasive quality of yeast strains with easy-to-understand steps to isolate the adhesion assessment from invasion assessment. Our method, adopted from previous studies, 10, 16 involves growing cells in liquid media and plating on differential nutrient conditions for growth of large spots, which we then wash with water to assess adhesion and rub cells completely off the agar surface to assess invasion into the agar. We eliminate the need for streaking cells onto agar, which affects the invasion of cells into the agar. In general, we observed that haploid strains that invade agar are always adhesive, yet not all adhesive strains can invade agar medium. Our approach can be used in conjunction with other assays to carefully dissect the differentiation steps and requirements of yeast signal transduction, differentiation, quorum sensing, and biofilm formation.

We describe a qualitative assay for yeast adhesion and agar invasion as a measure of invasive and pseudohyphal differentiation. This simple assay can be used to assess the invasive phenotype of various mutants as well as the effects environmental cues and signaling pathways on yeast differentiation.

Test di adesione ed invasione di Agar in S. cerevisiae

Yeasts are found in natural biofilms, where many microorganisms colonize surfaces. In artificial environments, such as surfaces of man-made objects, ...

Ricerca

Biologia

A high-throughput method to globally study the organelle morphology in S. cerevisiae

High-throughput methods to examine protein localization or organelle morphology is an effective tool for studying protein interactions and can help achieve an comprehensive understanding of molecular pathways. In Saccharomyces cerevisiae, with the development of the non-essential gene deletion array, we can globally study the morphology of different organelles like the endoplasmic reticulum (ER) and the mitochondria using GFP (or variant)-markers in different gene backgrounds. However, incorporating GFP markers in each single mutant individually is a labor-intensive process. Here, we describe a procedure that is routinely used in our laboratory. By using a robotic system to handle high-density yeast arrays and drug selection techniques, we can significantly shorten the time required and improve reproducibility. In brief, we cross a GFP-tagged mitochondrial marker (Apc1-GFP) to a high-density array of 4,672 nonessential gene deletion mutants by robotic replica pinning.  Through diploid selection, sporulation, germination and dual marker selection, we recover both alleles. As a result, each haploid single mutant contains Apc1-GFP incorporated at its genomic locus. Now, we can study the morphology of mitochondria in all non-essential mutant background. Using this high-throughput approach, we can conveniently study and delineate the pathways and genes involved in the inheritance and the formation of organelles in a genome-wide setting.

GFP-fusion proteins are widely used to visualize organelles by confocal microscopy. However, screening for mutations that affect the morphology of organelles generally requires individual mutagenesis and is time consuming. Here, we demonstrate a method to simultaneously incorporate organelle-GFP markers in almost 5,000 non-essential genes in yeast.

Un high-throughput metodo per studiare la morfologia globale organello in S. cerevisiae

High-throughput methods to examine protein localization or organelle morphology is an effective tool for studying protein interactions and can help ...

Quantitative Phosphoproteomics in Fatty Acid Stimulated Saccharomyces cerevisiae

This protocol describes the growth and stimulation, with the fatty acid oleate, of isotopically heavy and light S. cerevisiae cells. Cells are ground using a cryolysis procedure in a ball mill grinder and the resulting grindate brought into solution by urea solubilization. This procedure allows for the lysis of the cells in a metabolically inactive state, preserving phosphorylation and preventing reorientation of the phosphoproteome during cell lysis.  Following reduction, alkylation, trypsin digestion of the proteins, the samples are desalted on C18 columns and the sample complexity reduced by fractionation using hydrophilic interaction chromatography (HILIC). HILIC columns preferentially retain hydrophilic molecules which is well suited for phosphoproteomics.  Phosphorylated peptides tend to elute later in the chromatographic profile than the non phosphorylated counterparts. After fractionation, phosphopeptides are enriched using immobilized metal chromatography, which relies on charge-based affinities for phosphopeptide enrichment. At the end of this procedure the samples are ready to be quantitatively analyzed by mass spectrometry.

Quantitative Phosphoproteomics in Fatty Acid Stimulated Saccharomyces cerevisiae

Description of a quantitative phosphorylation procedure using cryolysis, urea solubilziation, HILIC fractionation and IMAC enrichment of phosphorylated peptides.

Fosfoproteomica quantitativa in acidi grassi Stimolati Saccharomyces cerevisiae</em

This protocol describes the growth and stimulation, with the fatty acid oleate, of isotopically heavy and light S. cerevisiae cells. Cells are ground ...

Studying Age-dependent Genomic Instability using the S. cerevisiae Chronological Lifespan Model

Studies using the Saccharomyces cerevisiae aging model have uncovered life span regulatory pathways that are partially conserved in higher eukaryotes1-2. The simplicity and power of the yeast aging model can also be explored to study DNA damage and genome maintenance as well as their contributions to diseases during aging. Here, we describe a system to study age-dependent DNA mutations, including base substitutions, frame-shift mutations, gross chromosomal rearrangements, and homologous/homeologous recombination, as well as nuclear DNA repair activity by combining the yeast chronological life span with simple DNA damage and mutation assays. The methods described here should facilitate the identification of genes/pathways that regulate genomic instability and the mechanisms that underlie age-dependent DNA mutations and cancer in mammals.

Studying Age-dependent Genomic Instability using the S. cerevisiae Chronological Lifespan Model

Here we describe a set of DNA mutation assays that can be combined with the yeast chronological life span model to study the genes/pathways that regulate or contribute to genomic DNA instability during aging.

Studiare età-dipendente instabilità genomica utilizzando il S. Saccharomyces Modello Durata cronologica

Studies using the Saccharomyces cerevisiae aging model have uncovered life span regulatory pathways that are partially conserved in higher eukaryotes1-2. ...

Identification of Protein Complexes in Escherichia coli using Sequential Peptide Affinity Purification in Combination with Tandem Mass Spectrometry

Since most cellular processes are mediated by macromolecular assemblies, the systematic identification of protein-protein interactions (PPI) and the identification of the subunit composition of multi-protein complexes can provide insight into gene function and enhance understanding of biological systems1, 2. Physical interactions can be mapped with high confidence vialarge-scale isolation and characterization of endogenous protein complexes under near-physiological conditions based on affinity purification of chromosomally-tagged proteins in combination with mass spectrometry (APMS). This approach has been successfully applied in evolutionarily diverse organisms, including yeast, flies, worms, mammalian cells, and bacteria1-6. In particular, we have generated a carboxy-terminal Sequential Peptide Affinity (SPA) dual tagging system for affinity-purifying native protein complexes from cultured gram-negative Escherichia coli, using genetically-tractable host laboratory strains that are well-suited for genome-wide investigations of the fundamental biology and conserved processes of prokaryotes1, 2, 7. Our SPA-tagging system is analogous to the tandem affinity purification method developed originally for yeast8, 9, and consists of a calmodulin binding peptide (CBP) followed by the cleavage site for the highly specific tobacco etch virus (TEV) protease and three copies of the FLAG epitope (3X FLAG), allowing for two consecutive rounds of affinity enrichment. After cassette amplification, sequence-specific linear PCR products encoding the SPA-tag and a selectable marker are integrated and expressed in frame as carboxy-terminal fusions in a DY330 background that is induced to transiently express a highly efficient heterologous bacteriophage lambda recombination system10. Subsequent dual-step purification using calmodulin and anti-FLAG affinity beads enables the highly selective and efficient recovery of even low abundance protein complexes from large-scale cultures. Tandem mass spectrometry is then used to identify the stably co-purifying proteins with high sensitivity (low nanogram detection limits).
Here, we describe detailed step-by-step procedures we commonly use for systematic protein tagging, purification and mass spectrometry-based analysis of soluble protein complexes from E. coli, which can be scaled up and potentially tailored to other bacterial species, including certain opportunistic pathogens that are amenable to recombineering. The resulting physical interactions can often reveal interesting unexpected components and connections suggesting novel mechanistic links. Integration of the PPI data with alternate molecular association data such as genetic (gene-gene) interactions and genomic-context (GC) predictions can facilitate elucidation of the global molecular organization of multi-protein complexes within biological pathways. The networks generated for E. coli can be used to gain insight into the functional architecture of orthologous gene products in other microbes for which functional annotations are currently lacking.

Identification of Protein Complexes in Escherichia coli using Sequential Peptide Affinity Purification in Combination with Tandem Mass Spectrometry

Affinity purification of tagged proteins in combination with mass spectrometry (APMS) is a powerful method for the systematic mapping of protein interaction networks and for investigating the mechanistic basis of biological processes. Here, we describe an optimized sequential peptide affinity (SPA) APMS procedure developed for the bacterium Escherichia coli that can be used to isolate and characterize stable multi-protein complexes to near homogeneity even starting from low copy numbers per cell.

Identificazione di complessi proteici in<em&gt; Escherichia coli</em&gt; Con sequenziale purificazione per affinità Peptide in combinazione con Tandem Mass Spectrometry

Since most cellular processes are mediated by macromolecular assemblies, the systematic identification of protein-protein interactions (PPI) and the ...

Flow Cytometry-based Purification of S. cerevisiae Zygotes

Zygotes are essential intermediates between haploid and diploid states in the life cycle of many organisms, including yeast (Figure 1) 1. S. cerevisiae zygotes result from the fusion of haploid cells of distinct mating type (MATa, MATalpha) and give rise to corresponding stable diploids that successively generate as many as 20 diploid progeny as a result of their strikingly asymmetric mitotic divisions 2. Zygote formation is orchestrated by a complex sequence of events: In this process, soluble mating factors bind to cognate receptors, triggering receptor-mediated signaling cascades that facilitate interruption of the cell cycle and culminate in cell-cell fusion. Zygotes may be considered a model for progenitor or stem cell function.
Although much has been learned about the formation of zygotes and although zygotes have been used to investigate cell-molecular questions of general significance, almost all studies have made use of mating mixtures in which zygotes are intermixed with a majority population of haploid cells 3-8. Many aspects of the biochemistry of zygote formation and the continuing life of the zygote therefore remain uninvestigated.
Reports of purification of yeast zygotes describe protocols based on their sedimentation properties 9; however, this sedimentation-based procedure did not yield nearly 90% purity in our hands. Moreover, it has the disadvantage that cells are exposed to hypertonic sorbitol. We therefore have developed a versatile purification procedure. For this purpose, pairs of haploid cells expressing red or green fluorescent proteins were co-incubated to allow zygote formation, harvested at various times, and the resulting zygotes were purified using a flow cytometry-based sorting protocol. This technique provides a convenient visual assessment of purity and maturation. The average purity of the fraction is approximately 90%. According to the timing of harvest, zygotes of varying degrees of maturity can be recovered. The purified samples provide a convenient point of departure for "-omic" studies, for recovery of initial progeny, and for systematic investigation of this progenitor cell.

Flow Cytometry-based Purification of S. cerevisiae Zygotes

To purify zygotes of S. cerevisiae, haploid cells of opposite mating type were engineered to express red or green fluorescent proteins, co-incubated to allow zygote formation, and fractionated using a flow cytometry-based protocol. The highly-enriched fraction enables subsequent "-omic" studies, recovery of initial progeny, and systematic investigation of zygote morphogenesis.

Flusso Cytometry basata Purificazione<em&gt; S. cerevisiae</em&gt; Zigoti

Zygotes are essential intermediates between haploid and diploid states in the life cycle of many organisms, including yeast (Figure 1) 1. S. cerevisiae ...

Visualization and Analysis of mRNA Molecules Using Fluorescence In Situ Hybridization in Saccharomyces cerevisiae

The Fluorescence in situ Hybridization (FISH) method allows one to detect nucleic acids in the native cellular environment. Here we provide a protocol for using FISH to quantify the number of mRNAs in single yeast cells. Cells can be grown in any condition of interest and then fixed and made permeable. Subsequently, multiple single-stranded deoxyoligonucleotides conjugated to fluorescent dyes are used to label and visualize mRNAs. Diffraction-limited fluorescence from single mRNA molecules is quantified using a spot-detection algorithm to identify and count the number of mRNAs per cell. While the more standard quantification methods of northern blots, RT-PCR and gene expression microarrays provide information on average mRNAs in the bulk population, FISH facilitates both the counting and localization of these mRNAs in single cells at single-molecule resolution.

Visualization and Analysis of mRNA Molecules Using Fluorescence In Situ Hybridization in Saccharomyces cerevisiae

This protocol describes an experimental procedure for performing Fluorescence in situ Hybridization (FISH) for counting mRNAs in single cells at single-molecule resolution.

Visualizzazione e l&#39;analisi di molecole di mRNA mediante fluorescenza<em&gt; In Situ</em&gt; Ibridazione in<em&gt; Saccharomyces cerevisiae</em

The Fluorescence in situ Hybridization (FISH) method allows one to detect nucleic acids in the native cellular environment. Here we provide a protocol for ...

Coupled Assays for Monitoring Protein Refolding in Saccharomyces cerevisiae

Proteostasis, defined as the combined processes of protein folding/biogenesis, refolding/repair, and degradation, is a delicate cellular balance that must be maintained to avoid deleterious consequences 1. External or internal factors that disrupt this balance can lead to protein aggregation, toxicity and cell death. In humans this is a major contributing factor to the symptoms associated with neurodegenerative disorders such as Huntington's, Parkinson's, and Alzheimer's diseases 10. It is therefore essential that the proteins involved in maintenance of proteostasis be identified in order to develop treatments for these debilitating diseases. This article describes techniques for monitoring in vivo protein folding at near-real time resolution using the model protein firefly luciferase fused to green fluorescent protein (FFL-GFP). FFL-GFP is a unique model chimeric protein as the FFL moiety is extremely sensitive to stress-induced misfolding and aggregation, which inactivates the enzyme 12. Luciferase activity is monitored using an enzymatic assay, and the GFP moiety provides a method of visualizing soluble or aggregated FFL using automated microscopy. These coupled methods incorporate two parallel and technically independent approaches to analyze both refolding and functional reactivation of an enzyme after stress. Activity recovery can be directly correlated with kinetics of disaggregation and re-solubilization to better understand how protein quality control factors such as protein chaperones collaborate to perform these functions. In addition, gene deletions or mutations can be used to test contributions of specific proteins or protein subunits to this process. In this article we examine the contributions of the protein disaggregase Hsp104 13, known to partner with the Hsp40/70/nucleotide exchange factor (NEF) refolding system 5, to protein refolding to validate this approach.

Coupled Assays for Monitoring Protein Refolding in Saccharomyces cerevisiae

This article describes the use of a firefly luciferase-GFP fusion protein to investigate in vivo protein folding in Saccharomyces cerevisiae. Using this reagent, refolding of a model heat-denatured protein can be monitored simultaneously by fluorescence microscopy and an enzymatic assay to probe the roles of proteostasis network components in protein quality control.

Saggi accoppiati per il monitoraggio delle proteine ​​in ripiegamento<em&gt; Saccharomyces cerevisiae</em

Proteostasis, defined as the combined processes of protein folding/biogenesis, refolding/repair, and degradation, is a delicate cellular balance that must ...

Identification of Post-translational Modifications of Plant Protein Complexes

Plants adapt quickly to changing environments due to elaborate perception and signaling systems. During pathogen attack, plants rapidly respond to infection via the recruitment and activation of immune complexes. Activation of immune complexes is associated with post-translational modifications (PTMs) of proteins, such as phosphorylation, glycosylation, or ubiquitination. Understanding how these PTMs are choreographed will lead to a better understanding of how resistance is achieved.
Here we describe a protein purification method for nucleotide-binding leucine-rich repeat (NB-LRR)-interacting proteins and the subsequent identification of their post-translational modifications (PTMs). With small modifications, the protocol can be applied for the purification of other plant protein complexes. The method is based on the expression of an epitope-tagged version of the protein of interest, which is subsequently partially purified by immunoprecipitation and subjected to mass spectrometry for identification of interacting proteins and PTMs.
This protocol demonstrates that: i). Dynamic changes in PTMs such as phosphorylation can be detected by mass spectrometry; ii). It is important to have sufficient quantities of the protein of interest, and this can compensate for the lack of purity of the immunoprecipitate; iii). In order to detect PTMs of a protein of interest, this protein has to be immunoprecipitated to get a sufficient quantity of protein.

We describe here a protocol for the purification and characterization of plant protein complexes. We demonstrate that by immunoprecipitating a single protein within a complex, so we can identify its post-translational modifications and its interacting partners.

Identificazione delle modificazioni post-traduzionali di proteine ​​vegetali Complessi

Plants adapt quickly to changing environments due to elaborate perception and signaling systems. During pathogen attack, plants rapidly respond to ...

Identification of Protein Interaction Partners in Mammalian Cells Using SILAC-immunoprecipitation Quantitative Proteomics

Quantitative proteomics combined with immuno-affinity purification, SILAC immunoprecipitation, represent a powerful means for the discovery of novel protein:protein interactions. By allowing the accurate relative quantification of protein abundance in both control and test samples, true interactions may be easily distinguished from experimental contaminants. Low affinity interactions can be preserved through the use of less-stringent buffer conditions and remain readily identifiable. This protocol discusses the labeling of tissue culture cells with stable isotope labeled amino acids, transfection and immunoprecipitation of an affinity tagged protein of interest, followed by the preparation for submission to a mass spectrometry facility. This protocol then discusses how to analyze and interpret the data returned from the mass spectrometer in order to identify cellular partners interacting with a protein of interest. As an example this technique is applied to identify proteins binding to the eukaryotic translation initiation factors: eIF4AI and eIF4AII.

SILAC immunoprecipitation experiments represent a powerful means for discovering novel protein:protein interactions. By allowing the accurate relative quantification of protein abundance in both control and test samples, true interactions may be easily distinguished from experimental contaminants, and low affinity interactions preserved through use of less-stringent buffer conditions.

Identificazione delle proteine ​​partner di interazione in cellule di mammifero Uso SILAC-immunoprecipitazione quantitativi Proteomica

Quantitative proteomics combined with immuno-affinity purification, SILAC immunoprecipitation, represent a powerful means for the discovery of novel ...